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Page 1
Intrachromosomal triplication for the distal part of chromosome 15q.
Schluth C, Mattei MG, Mignon-Ravix C, Salman S, Alembik Y, Willig J, Ginglinger E, Jeandidier E. Schluth C, et al. Among authors: jeandidier e. Am J Med Genet A. 2005 Jul 15;136(2):179-84. doi: 10.1002/ajmg.a.30745. Am J Med Genet A. 2005. PMID: 15940678 Review.
Validation of image processing tools for 3-D fluorescence microscopy.
Dieterlen A, Xu C, Gramain MP, Haeberlé O, Colicchio B, Cudel C, Jacquey S, Ginglinger E, Jung G, Jeandidier E. Dieterlen A, et al. Among authors: jeandidier e. C R Biol. 2002 Apr;325(4):327-34. doi: 10.1016/s1631-0691(02)01448-8. C R Biol. 2002. PMID: 12161912 Free article.
Phenotype in X chromosome rearrangements: pitfalls of X inactivation study.
Schluth C, Cossée M, Girard-Lemaire F, Carelle N, Dollfus H, Jeandidier E, Flori E. Schluth C, et al. Among authors: jeandidier e. Pathol Biol (Paris). 2007 Feb;55(1):29-36. doi: 10.1016/j.patbio.2006.04.003. Epub 2006 May 11. Pathol Biol (Paris). 2007. PMID: 16690229
A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity.
Jeandidier E, Gervais C, Radford-Weiss I, Zink E, Gangneux C, Eischen A, Galoisy AC, Helias C, Dano L, Cammarata O, Jung G, Harzallah I, Guérin E, Martzolff L, Drénou B, Lioure B, Tancrédi C, Rimelen V, Mauvieux L. Jeandidier E, et al. Cancer Genet. 2012 Jul-Aug;205(7-8):365-72. doi: 10.1016/j.cancergen.2012.04.007. Cancer Genet. 2012. PMID: 22867997
Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Français de Cytogénétique Hématologique.
Jeandidier E, Dastugue N, Mugneret F, Lafage-Pochitaloff M, Mozziconacci MJ, Herens C, Michaux L, Verellen-Dumoulin C, Talmant P, Cornillet-Lefebvre P, Luquet I, Charrin C, Barin C, Collonge-Rame MA, Pérot C, Van den Akker J, Grégoire MJ, Jonveaux P, Baranger L, Eclache-Saudreau V, Pagès MP, Cabrol C, Terré C, Berger R; Groupe Français de Cytogénétique Hématologique (GFCH). Jeandidier E, et al. Cancer Genet Cytogenet. 2006 Apr 1;166(1):1-11. doi: 10.1016/j.cancergencyto.2005.08.005. Cancer Genet Cytogenet. 2006. PMID: 16616106
A Central Role of Telomere Dysfunction in the Formation of a Unique Translocation within the Sub-Telomere Region Resulting in Duplication and Partial Trisomy.
M'Kacher R, Miguet M, Maillard PY, Colicchio B, Scheidecker S, Najar W, Arnoux M, Oudrhiri N, Borie C, Biehler M, Plesch A, Heidingsfelder L, Bennaceur-Griscelli A, Dieterlen A, Voisin P, Junker S, Carde P, Jeandidier E. M'Kacher R, et al. Among authors: jeandidier e. Genes (Basel). 2022 Sep 29;13(10):1762. doi: 10.3390/genes13101762. Genes (Basel). 2022. PMID: 36292646 Free PMC article.
Telomere and Centromere Staining Followed by M-FISH Improves Diagnosis of Chromosomal Instability and Its Clinical Utility.
M'kacher R, Colicchio B, Borie C, Junker S, Marquet V, Heidingsfelder L, Soehnlen K, Najar W, Hempel WM, Oudrhiri N, Wilhelm-Murer N, Miguet M, Arnoux M, Ferrapie C, Kerbrat W, Plesch A, Dieterlen A, Girinsky T, Voisin P, Deschenes G, Tabet AC, Yardin C, Bennaceur-Griscelli A, Fenech M, Carde P, Jeandidier E. M'kacher R, et al. Among authors: jeandidier e. Genes (Basel). 2020 Apr 27;11(5):475. doi: 10.3390/genes11050475. Genes (Basel). 2020. PMID: 32349350 Free PMC article.
Telomere aberrations, including telomere loss, doublets, and extreme shortening, are increased in patients with infertility.
M'kacher R, Colicchio B, Marquet V, Borie C, Najar W, Hempel WM, Heidingsfelder L, Oudrhiri N, Al Jawhari M, Wilhelm-Murer N, Miguet M, Dieterlen A, Deschênes G, Tabet AC, Junker S, Grynberg M, Fenech M, Bennaceur-Griscelli A, Voisin P, Carde P, Jeandidier E, Yardin C. M'kacher R, et al. Among authors: jeandidier e. Fertil Steril. 2021 Jan;115(1):164-173. doi: 10.1016/j.fertnstert.2020.07.005. Epub 2020 Dec 4. Fertil Steril. 2021. PMID: 33272625 Free article.
44 results